Newborn genomic screening may detect hundreds of additional childhood conditions
Tehnologie
Murdoch Childrens Research Institute Oct 9 2025 Adding genomic sequencing to newborn blood screening would detect hundreds of additional childhood conditions, providing much earlier diagnosis and treatment, according to a new study. A baby's genome, which stays with them for life, could also be re-examined if a health issue arises during their lifetime. The study, led by Murdoch Children's Research Institute (MCRI) and Victorian Clinical Genetics Services (VCGS), found genomic screening, a test
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